510(k) K083510 ยท KPR System, X-Ray, Stationary
KUBTEC XPERT 20
| Applicant | Kub Technologies, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jan 8, 2009 |
| Received | Nov 26, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083510
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.